Following a brief description of the historical and genetic background of the condition HMS is described in relation to other connective tissue disorders, such as Ehlers-Danlos syndrome, the Marfan Syndrome etc. The hypermobility syndrome is distinct ...view more
Following a brief description of the historical and genetic background of the condition HMS is described in relation to other connective tissue disorders, such as Ehlers-Danlos syndrome, the Marfan Syndrome etc. The hypermobility syndrome is distinct from hypermobility (as in one joint only), which most physiotherapists are familiar with, and this difference will be explored. Hypermobility, is something people are born with, but it does not necessarily produce symptoms. It is present in between 5-15% of the population. Many of these will suffer symptoms at some stage in their life. It may occur in childhood, adolescence, adulthood, pregnancy or old age. Each of these stages is covered in the book, with detailed information on the presentation of the condition and its management. There are contributions from a variety of medical practitioners experienced in this field:. Consultant Rheumatologist, Professor R Grahame, Consultant Paediatrician, Dr K Murray, GP, Dr E Mansi, several physiotherapists, who specialise in different areas; Rosemary Keer (adults), Alison Middleditch (adolescents), Vicky Harding (Chronic pain), Jane Simmonds (Rehabilitation) & Sue Maillard (paediatric). There will also be a contribution from Sarah Gurley-Green, past Chairperson to the Hypermobility Syndrome association.
Following a brief description of the historical and genetic background of the condition HMS is described in relation to other connective tissue disorders, such as Ehlers-Danlos syndrome, the Marfan Syndrome etc. The hypermobility syndrome is distinct from hypermobility (as in one joint only), which most physiotherapists are familiar with, and this difference will be explored. Hypermobility, is something people are born with, but it does not necessarily produce symptoms. It is present in between 5-15% of the population. Many of these will suffer symptoms at some stage in their life. It may occur in childhood, adolescence, adulthood, pregnancy or old age. Each of these stages is covered in the book, with detailed information on the presentation of the condition and its management. There are contributions from a variety of medical practitioners experienced in this field:. Consultant Rheumatologist, Professor R Grahame, Consultant Paediatrician, Dr K Murray, GP, Dr E Mansi, several physiotherapists, who specialise in different areas; Rosemary Keer (adults), Alison Middleditch (adolescents), Vicky Harding (Chronic pain), Jane Simmonds (Rehabilitation) & Sue Maillard (paediatric). There will also be a contribution from Sarah Gurley-Green, past Chairperson to the Hypermobility Syndrome association.
Key Features
Demonstrates how to identify the condition in the clinic.
Discusses treatment and management strategies.
Provides examples in the form of case studies.
Includes details of a comprehensive assessment procedure, which differs depending on the stage of the disorder and the age of the patient.
Features contributions by experts in a range of medical fields.
Author Information
By Rosemary J. Keer, MSc, MCSP, MACP, Specialist Chartered Physiotherapist, Central London Physiotherapy Clinic, Harley Street, London UK and Rodney Grahame, CBE, MD, FRCP, FACP, Consultant Rheumatologist, University College Hospital, London, UK
1. Hypermobility and Hypermobility syndrome2. Hypermobility and the Heritable Disorders of Connective Tissue3. Overall Management of the Joint Hypermobility Syndrome 4. Hypermobility Syndrome in Children5. Management of the Hypermobile Adolescent6. Physiotherapy Assessment of the Hypermobile Adult7. Management of the Hypermobile Adult 8. Rehabilitation, Fitness, Sport and Performance for Individuals with Joint Hypermobility 9. Joint Hypermobility and Work Related Musculoskeletal Disorders (WMSD)10. Joint Hypermobility and Chronic Pain: Possible Linking Mechanisms and Management Highlighted by a Cognitive-Behavioural Approach.11. Hypermobility Syndrome from the Patient's Perspective
https://www.us.elsevierhealth.com/hypermobility-syndrome-9780750653909.html5688Hypermobility Syndromehttps://www.us.elsevierhealth.com/media/catalog/product/9/7/9780750653909.jpg62.3677.95USDInStock/Health Professions/Physical Therapy and Rehabilitation/Books/Winter Sale - 20% Off Select Books and eBooks22525503959246531365145120Following a brief description of the historical and genetic background of the condition HMS is described in relation to other connective tissue disorders, such as Ehlers-Danlos syndrome, the Marfan Syndrome etc. The hypermobility syndrome is distinct from hypermobility (as in one joint only), which most physiotherapists are familiar with, and this difference will be explored. Hypermobility, is something people are born with, but it does not necessarily produce symptoms. It is present in between 5-15% of the population. Many of these will suffer symptoms at some stage in their life. It may occur in childhood, adolescence, adulthood, pregnancy or old age. Each of these stages is covered in the book, with detailed information on the presentation of the condition and its management. There are contributions from a variety of medical practitioners experienced in this field:. Consultant Rheumatologist, Professor R Grahame, Consultant Paediatrician, Dr K Murray, GP, Dr E Mansi, several physiotherapists, who specialise in different areas; Rosemary Keer (adults), Alison Middleditch (adolescents), Vicky Harding (Chronic pain), Jane Simmonds (Rehabilitation) & Sue Maillard (paediatric). There will also be a contribution from Sarah Gurley-Green, past Chairperson to the Hypermobility Syndrome association. Following a brief description of the historical and genetic background of the condition HMS is described in relation to other connective tissue disorders, such as Ehlers-Danlos syndrome, the Marfan Syndrome etc. The hypermobility syndrome is distinct from hypermobility (as in one joint only), which most physiotherapists are familiar with, and this difference will be explored. Hypermobility, is something people are born with, but it does not necessarily produce symptoms. It is present in between 5-15% of the population. Many of these will suffer symptoms at some stage in their life. It may occur in childhood, adolescence, adulthood, pregnancy or old age. Each of these stages is covered in the book, with detailed information on the presentation of the condition and its management. There are contributions from a variety of medical practitioners experienced in this field:. Consultant Rheumatologist, Professor R Grahame, Consultant Paediatrician, Dr K Murray, GP, Dr E Mansi, several physiotherapists, who specialise in different areas; Rosemary Keer (adults), Alison Middleditch (adolescents), Vicky Harding (Chronic pain), Jane Simmonds (Rehabilitation) & Sue Maillard (paediatric). There will also be a contribution from Sarah Gurley-Green, past Chairperson to the Hypermobility Syndrome association.00add-to-cart97807506539092011 and earlierProfessionalBy Rosemary J. Keer, MSc, MCSP, MACP and Rodney Grahame, CBE, MD, FRCP, FACP20031Book189w x 246h (7.44" x 9.68")Butterworth-Heinemann188Jun 26, 2003IN STOCK - This may take up to 5 business days to shipBy <STRONG>Rosemary J. Keer</STRONG>, MSc, MCSP, MACP, Specialist Chartered Physiotherapist, Central London Physiotherapy Clinic, Harley Street, London UK and <STRONG>Rodney Grahame</STRONG>, CBE, MD, FRCP, FACP, Consultant Rheumatologist, University College Hospital, London, UKBooksBooksNoNoNoNoPlease SelectPlease SelectPlease Select
